Publication | Closed Access
Aldol Reaction under Solvent-Free Conditions: Highly Stereoselective Synthesis of 1,3-Amino Alcohols
58
Citations
15
References
2000
Year
EngineeringBiochemistryNatural SciencesDiversity-oriented Synthesis1,3-Amino AlcoholsRemote SubstituentOrganic ChemistrySolvent-free ConditionsSynthetic ChemistryStereoselective SynthesisChemistryHigh SelectivityAsymmetric CatalysisAldol ReactionEnantioselective SynthesisBiomolecular Engineering
[formula: see text] A method for the highly stereoselective synthesis of 1,3-amino alcohols based on the indium trichloride-catalyzed Mukaiyama aldol reaction of keto ester (R,S)-1 under solvent-free conditions has been developed. The high selectivity observed can be explained on the basis of the shielding of one face by a remote substituent.
| Year | Citations | |
|---|---|---|
Page 1
Page 1